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Here the simulation study setting is defined.
id <- 1
onset <- 3
a0 <- 2
a1 <- 3
refDose <- 56
# True dose-DLT relationship
myTruth <- function(dose) {
StandLogDose <- log(dose / refDose)
plogis(a0 + a1 * StandLogDose)
}
# The conditional CDF of the PEM
if (onset == 30) {
onset <- 15
exp_cond_cdf <- function(x) {
(pexp(42 - x, 1 / onset, lower.tail = FALSE) - pexp(t_max, 1 / onset, lower.tail = FALSE)) / pexp(t_max, 1 / onset)
}
} else {
exp_cond_cdf <- function(x) {
1 - (pexp(x, 1 / onset, lower.tail = FALSE) - pexp(t_max, 1 / onset, lower.tail = FALSE)) / pexp(t_max, 1 / onset)
}
}Here the the dose escalation designs are defined: in this example the
TITE-CRM is used. Similarly the code can be adapted for the rolling-CRM
which is implemented in DALogisticLogNormal. Note that
another alternative is TITELogisticLogNormalSub which is a
submodel of LogisticLogNormalSub, which uses again the
subtraction of the reference dose from the dose level in the regression
model.
library(crmPack)
t_max <- 42
model <- TITELogisticLogNormal(
mean = c(1.33, 1.49),
cov = matrix(c(1.826, 0.0209, 0.0209, 0.0245), nrow = 2),
ref_dose = refDose
)
myIncrements <- IncrementsRelative(
intervals = c(0, 20),
increments = c(10, 3)
)
myNextBest <- NextBestMTD(
target = 0.3,
derive =
function(mtd_samples) {
mean(mtd_samples)
}
)
myStopping <- StoppingMinPatients(nPatients = 48)
mySize <- CohortSizeConst(size = 3)
emptydata <- DataDA(doseGrid = seq(from = 2, to = 50, by = 2), Tmax = t_max)
mysafetywindow <- SafetyWindowConst(c(7, 7), 7, 7)
design <- DADesign(
model = model,
increments = myIncrements,
nextBest = myNextBest,
stopping = myStopping,
cohort_size = mySize,
data = emptydata,
safetyWindow = mysafetywindow,
startingDose = 8
)In order to obtain stable results, increase the simulation parameters appropriately (step, samples, nsim).
These binaries (installable software) and packages are in development.
They may not be fully stable and should be used with caution. We make no claims about them.